Canonical Allele Identifier: CA1398327353

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284456A= , CM000665.2:g.123284456A=	GRCh38
NC_000003.11:g.123003303A= , CM000665.1:g.123003303A=	GRCh37
NC_000003.10:g.124485993A=	NCBI36
NG_033882.1:g.169090T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000466617.6:c.*152T=	ENSP00000420082.2:n.*152T=
ENST00000470367.2:c.*152T=	ENSP00000514541.1:n.*152T=
ENST00000483566.2:c.*152T=	ENSP00000420252.2:n.*152T=
ENST00000699714.1:c.*152T=	ENSP00000514539.1:n.*152T=
ENST00000699715.1:c.*152T=	ENSP00000514540.1:n.*152T=
ENST00000699716.1:c.*152T=	ENSP00000514542.1:n.*152T=
ENST00000699717.1:n.2341T=
ENST00000699718.1:c.4013T=	ENSP00000514543.1:n.4013T=
ENST00000462833.6:c.*152T= MANE Select	ENSP00000419361.1:n.*152T=
ENST00000462833.5:c.*152T=	ENSP00000419361.1:n.*152T=
ENST00000478092.1:n.708T=
ENST00000491190.5:c.*152T=	ENSP00000418537.1:n.*152T=
NM_001199642.1:c.*152T=	NP_001186571.1:n.*152T=
NM_183357.2:c.3938T=	NP_899200.1:n.3938T=
XM_005247077.2:c.*152T=	XP_005247134.1:n.*152T=
XM_005247078.1:c.*152T=	XP_005247135.1:n.*152T=
XM_006713483.1:c.*152T=	XP_006713546.1:n.*152T=
XM_006713484.1:c.*152T=	XP_006713547.1:n.*152T=
XM_011512359.1:c.*152T=	XP_011510661.1:n.*152T=
XM_011512360.1:c.*152T=	XP_011510662.1:n.*152T=
XM_011512361.1:c.*152T=	XP_011510663.1:n.*152T=
XM_005247077.4:c.*152T=	XP_005247134.1:n.*152T=
XM_011512359.2:c.*152T=	XP_011510661.1:n.*152T=
XM_011512360.3:c.*152T=	XP_011510662.1:n.*152T=
XM_017005638.1:c.*152T=	XP_016861127.1:n.*152T=
XM_017005639.1:c.*152T=	XP_016861128.1:n.*152T=
NM_001378259.1:c.*152T=	NP_001365188.1:n.*152T=
NM_183357.3:c.*152T= MANE Select	NP_899200.1:n.*152T=